Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001267580.1 | 1693 | Silent Mutation | GCA,GCG | A517A | NP_001254509.1 |
NM_003981.3 | 1693 | Missense Mutation | CAA,CGA | Q598R | NP_003972.1 |
NM_199413.2 | 1693 | Missense Mutation | CAA,CGA | Q584R | NP_955445.1 |
XM_005254987.2 | 1693 | Silent Mutation | GCA,GCG | A558A | XP_005255044.1 |
XM_006720759.1 | 1693 | UTR 3 | XP_006720822.1 | ||
XM_006720760.1 | 1693 | Intron | XP_006720823.1 | ||
XM_011522187.1 | 1693 | Intron | XP_011520489.1 | ||
XM_011522188.2 | 1693 | Intron | XP_011520490.1 | ||
XM_011522189.1 | 1693 | Intron | XP_011520491.1 | ||
XM_011522190.2 | 1693 | Intron | XP_011520492.1 | ||
XM_011522191.2 | 1693 | Intron | XP_011520493.1 | ||
XM_011522192.1 | 1693 | Intron | XP_011520494.1 | ||
XM_017022712.1 | 1693 | Missense Mutation | CAA,CGA | Q561R | XP_016878201.1 |
XM_017022713.1 | 1693 | Missense Mutation | CAA,CGA | Q547R | XP_016878202.1 |
XM_017022714.1 | 1693 | Intron | XP_016878203.1 | ||
XM_017022715.1 | 1693 | Missense Mutation | CAA,CGA | Q546R | XP_016878204.1 |
XM_017022716.1 | 1693 | Missense Mutation | CAA,CGA | Q527R | XP_016878205.1 |
XM_017022717.1 | 1693 | Silent Mutation | GCA,GCG | A506A | XP_016878206.1 |